Wild-Type Transthyretin Amyloid Depositions in the Subcutaneous Fat and Skeletal Muscles of a Nonagenarian Who Had Heart Failure With Preserved Ejection Fraction and No Myocardial Technetium-99m-Labeled Pyrophosphate Uptake. [PDF]
Takahashi K+4 more
europepmc +1 more source
Cytological Assessment of Adrenal Tumours: Insights From 22‐Years Single Centre Experience
ABSTRACT Objective The incidence of adrenal tumours has increased in the last decades, mainly due to increased use of imaging. The diagnostic evaluation of adrenal masses can be complex and, in some cases, necessitates cytological evaluation. However, concerns remain regarding the potential complications associated with adrenal gland biopsy.
Ana Carasel+3 more
wiley +1 more source
Amyloidosis in Human Inborn Errors of Immunity Predicts Poor Prognosis. [PDF]
Aytekin ES+7 more
europepmc +1 more source
Clinical and Clinico-Pathological Observations of Generalized Amyloidosis in Cattle
Tatsuo Konishi+2 more
openalex +2 more sources
Abstract Background The validation of a combination of plasma biomarkers and demographic variables is required to establish reliable cut‐offs for Alzheimer's disease diagnosis (AD). Methods Plasma biomarkers (Aβ42/Aβ40, p‐Tau181, t‐Tau, NfL, GFAP), ApoE genotype, and demographic variables were obtained from a retrospective clinical cohort of cognitive ...
Lourdes Álvarez‐Sánchez+8 more
wiley +1 more source
Light Chain (AL) Amyloidosis Masquerading as Scleroderma: A Diagnostic Challenge. [PDF]
Dhamija K+4 more
europepmc +1 more source
This consensus highlights critical research gaps in obesity epidemiology, phenotypic heterogeneity and clinical management, calling for advanced methodologies, collaborative strategies and innovative policies to mitigate the global obesity epidemic and its socio‐economic impacts.
Federico Carbone+28 more
wiley +1 more source
Diffuse lung involvement as a rare presentation of systemic AL amyloidosis: a retrospective cohort study. [PDF]
Song A+14 more
europepmc +1 more source
The Spectrum of Epidermolysis Bullosa in KwaZulu‐Natal, South Africa
ABSTRACT Background Epidermolysis bullosa (EB) is a rare, heterogeneous genodermatosis characterized by skin fragility due to inherited defects in genes encoding proteins that maintain epidermal–dermal integrity. The severity and complications of EB vary by subtype, and no cure currently exists. The epidemiology is unknown in South Africa. Methods This
Antoinette Chateau+10 more
wiley +1 more source
Screening for Cardiac Amyloidosis When Conducting Carpal Tunnel Surgery. [PDF]
Pimenta S+15 more
europepmc +1 more source